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作 者:刘斌[1] 易永芬[1] 李园园[1] 廖晓刚[2]
机构地区:[1]重庆医科大学基础医学院病理学教研室 [2]重庆医科大学基础医学院电镜教研室,重庆400016
出 处:《重庆医科大学学报》2003年第6期825-827,830,共4页Journal of Chongqing Medical University
摘 要:目的 :提高对小儿胆道胚胎型横纹肌肉瘤 (葡萄状肉瘤 )的认识 ,减少误诊。方法 :对本病例及国内文献报道的胆道胚胎型横纹肌肉瘤 (葡萄状肉瘤 )病例共 16例进行分析。结果 :男 11例 ,女 5例。年龄 1~ 6岁。黄疸 16例 ,发热 8例 ,右上腹痛 6例 ,陶土色大便 9例 ,尿黄 6例。肝肿大 13例 ,脾肿大 2例 ,右上腹肿块 2例。临床误诊为肝炎 5例。B超考虑葡萄状肉瘤仅 2例 ,CT考虑胆总管横纹肌肉瘤仅 1例。病检诊断 :胚胎型横纹肌肉瘤 3例 ,葡萄状肉瘤 13例。 7例切除并化疗、放疗 ,随访最长的 8个月未复发。 1例部分切除并化疗 ,3个月后随访残留灶缩小 ,病情稳定。 2例行姑息手术后 2个月左右死亡。 1例切除后 2个月检查已复发。结论 :小儿胆道横纹肌肉瘤为胚胎型横纹肌肉瘤 (葡萄状肉瘤 ) ,发病年龄 1~ 6岁 ,男性比女性多见。其主要症状为阻塞性黄疸 ,常伴有发热、肝肿大等 ,临床易误诊为肝炎。B超、CT等辅助检查有助于诊断 ,确诊需经病理检查。本病恶性程度高 ,预后差 ,应积极外科治疗并配合化疗、放疗 ,可延长生存时间。Objective:To improve the understanding and diagnosis of embryonal rhabdomysarcoma of biliary tree in childhood.Methods:The management of 1 child with sarcoma botryoides of biliary tree and other 15 cases reported were reviewed.Results:11 cases of boys and 5 of girls,varying from 1 to 6 years old.Clinical symptoms at presentation included jaundice in 16/16,fever 8/16,abdominal pain 6/16,white feces 9/16 and hepatomegaly 13/16, etc.5 cases of which were misdiagnosed as having hepatitis.There were only 2 cases considered as rhabdomyosarcoma by ultrasound and 1 by abdominal CT scan.7 cases had not recurred in 8 months after combined treatment of complete surgical excision,chemotherapy and radiotherapy.Treated with combination of partial excision and chemotherapy,1 case's tumor turned smaller 3 months later.But 2 cases treated solely with partial excision died 2 months later and 1 case recurred 2 months later.Conclusion:All rhabdomyosarcoma of biliary tree in childhood are botryoid,embryonal rhabdomyosarcoma.The patients are aged from 1 to 6 years old,and boys are more common than girls.The main clinical symptoms are obstructive jaundice,fever and hepatomegaly,so it is easily misdiagnosed as hepatitis in clinic.Ultrasound and abdominal CT sacn are helpful in diagnosing embryonal rhabdomysarcoma (sarcoma botryoides) of biliary tree,but pathological examination is essential for confirming the disease.A combined approach of aggressive surgery,chemotherapy and radiotherapy may result in long-term survival.
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